PDE10 inhibitors and related compositions and methods
Isolated or pure compounds that inhibit PDE10 are disclosed that have utility in the treatment of a variety of conditions, including but not limited to psychotic, anxiety, movement disorders and/or neurological disorders such as Parkinson's disease, Huntington's disease, Alzheimer's disease, encephalitis, phobias, epilepsy, aphasia, Bell's palsy, cerebral palsy, sleep disorders, pain, Tourette's syndrome, schizophrenia, delusional disorders, drug-induced psychosis and panic and obsessive-compulsive disorders. Pharmaceutically acceptable salts, stereoisomers, solvates and prodrugs of the compounds are also provided. Also disclosed are compositions containing an isolated or pure compound in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for inhibiting PDE10 in a warm-blooded animal in need of the same.
1. An isolated compound of the following structure (I):
or a pharmaceutically acceptable salt, stereoisomer, or solvate thereof, wherein:
R 1 is H, C 1-3 alkyl, hydroxy-C 1-3 alkyl, C 1-3 alkoxy, C 1-3 alkyl-O-glucuronidyl;
R 2 is H, ethyl, or glucuronidyl;
R 3 and R 4 are each independently H, C 1-3 alkyl, or glucuronidyl; and
X is ═O, —OH or —O-glucuronidyl,
with the proviso that said compound of structure (I) is not:
2. The isolated compound of claim 1 , wherein R 1 is methyl or hydroxymethyl.
3. The isolated compound of claim 1 , wherein R 2 is ethyl.
4. The isolated compound of claim 1 , wherein R 3 and R 4 are each independently H, methyl, or glucuronidyl.
5. The isolated compound of claim 1 , wherein X is ═O or —OH.
6. The isolated compound of claim 1 , wherein the compound is selected from the group consisting of:
7. A compound of the following structure (I):
or a pharmaceutically acceptable salt, stereoisomer, or solvate thereof, wherein:
R 1 is H, C 1-3 alkyl, hydroxy-C 1-3 alkyl, C 1-3 alkoxy, C 1-3 alkyl-O-glucuronidyl;
R 2 is H, ethyl, or glucuronidyl;
R 3 and R 4 are each independently H, C 1-3 alkyl, or glucuronidyl; and
X is ═O, —OH or —O-glucuronidyl,
with the proviso that said compound of structure (I) is not:
wherein the purity of the compound is 98% or higher.
8. The compound of claim 7 , wherein R 1 is methyl or hydroxymethyl.
9. The compound of claim 7 , wherein R 2 is ethyl.
10. The compound of claim 7 , wherein R 3 and R 4 are each independently H, methyl, or glucuronidyl.
11. The compound of claim 7 , wherein X is ═O or —OH.
12. The compound of claim 7 , wherein the compound is selected from the group consisting of:
13. The compound of claim 7 , wherein the purity of the compound is 98.5% or higher.
14. The compound of claim 7 , wherein the purity of the compound is 99% or higher.
15. The compound of claim 7 , wherein the purity of the compound is 99.5% or higher.
16. A pharmaceutical composition comprising the isolated compound of claim 1 and at least one pharmaceutically acceptable carrier or diluent.
17. A pharmaceutical composition comprising the compound of claim 7 and at least one pharmaceutically acceptable carrier or diluent.
18. A method for inhibiting PDE10 in a warm-blooded animal, comprising administering to the animal an effective amount of an isolated compound of claim 1 or a pharmaceutical composition of claim 16 .
19. A method for inhibiting PDE10 in a warm-blooded animal, comprising administering to the animal an effective amount of a compound of claim 7 or a pharmaceutical composition of claim 17 .
20. A method for treating neurological disorders in a warm-blooded animal in need thereof, comprising administering to the animal an effective amount of an isolated compound of claim 1 or a pharmaceutical composition of claim 16 .
21. A method for treating neurological disorders in a warm-blooded animal in need thereof, comprising administering to the animal an effective amount of a compound of claim 7 or a pharmaceutical composition of claim 17 .
22. The method of claim 20 , wherein the neurological disorder is selected from the group consisting of psychotic disorders, anxiety disorders, Parkinson's disease, Huntington's disease, Alzheimer's disease, encephalitis, phobias, epilepsy, aphasia, Bell's palsy, cerebral palsy, sleep disorders, pain, Tourette's syndrome, schizophrenia, delusional disorders, bipolar disorders, posttraumatic stress disorders, drug-induced psychosis, panic disorders, obsessive-compulsive disorders, attention-deficit disorders, disruptive behavior disorders, autism, depression, dementia, epilepsy, insomnias, and multiple sclerosis.
23. The method of claim 22 , wherein the neurological disorder is schizophrenia.
24. The method of claim 22 , wherein the neurological disorder is post-traumatic stress disorder.
25. The method of claim 22 , wherein the neurological disorder is Huntington's disease.
26. The method of claim 21 , wherein the neurological disorder is selected from the group consisting of psychotic disorders, anxiety disorders, Parkinson's disease, Huntington's disease, Alzheimer's disease, encephalitis, phobias, epilepsy, aphasia, Bell's palsy, cerebral palsy, sleep disorders, pain, Tourette's syndrome, schizophrenia, delusional disorders, bipolar disorders, posttraumatic stress disorders, drug-induced psychosis, panic disorders, obsessive-compulsive disorders, attention-deficit disorders, disruptive behavior disorders, autism, depression, dementia, epilepsy, insomnias, and multiple sclerosis.
27. The method of claim 26 , wherein the neurological disorder is schizophrenia.
28. The method of claim 26 , wherein the neurological disorder is post-traumatic stress disorder.
29. The method of claim 26 , wherein the neurological disorder is Huntington's disease.